ライフサイエンスコーパス: keyhole

1 comes chaotic following transition to a full keyhole.

2 with low enough power to avoid generating a keyhole.

3 minant mechanism controlling flow behind the keyhole.

4 s near the keyhole tip to move away from the keyhole and become trapped as defects.

5 Using synchrotron X-ray imaging we reveal keyhole and bubble behaviour, quantifying their formatio

6 liminating the balling and sparring effects, keyhole and cavity formation by attaining effective melt

7 Postcontrast keyhole and half-Fourier images were formed from the sam

8 y across several parameter sets by analysing keyhole and plume morphologies, and identify a previousl

9 Keyhole number, to predict aspect ratio of a keyhole and the morphological transition from stable at

10 amics with high-energy x-rays shows that (i) keyholes are present across the range of power and scann

11 ., lack of fusions, gas-entrapped pores, and keyholes, are quantified by nine parameters including ma

12 ll-defined threshold from conduction mode to keyhole based on laser power density; and (iii) the tran

13 and laser powder bed fusion (LPBF) can cause keyhole collapse and pore formation.

14 p the rear-wall; and (iii) immediately after keyhole collapse, bubbles undergo rapid growth due to pr

15 The channel, which is shaped like a keyhole, contains several distinct nucleoside-binding si

16 to the rapid formation then collapse of deep keyhole depressions in the surface which traps inert shi

17 enomenon of vapor depressions (also known as keyholes) during laser melting of metals as practiced in

18 7 x 2.5-mm spatial resolution, 4 seconds per keyhole dynamic frame) was obtained over 90 seconds befo

19 The keyhole fluctuation and bubble evolution mechanisms reve

20 keyhole porosity formation mechanisms, e.g., keyhole fluctuation, collapse and bubble growth and shri

21 wer-velocity conditions, causing fast radial keyhole fluctuations (2.5-10 kHz); (ii) transition regim

22 eams significantly reduce the propensity for keyhole formation across a broad scan parameter space.

23 e liquid surface, instability, and then deep keyhole formation.

24 curs when an unstable vapor depression zone (keyhole) forms because of excess laser energy input.

25 The nESI source incorporates a keyhole geometry ion funnel design which facilitates axi

26 nsistently emphasised structures such as the keyhole in Fissurella volcano and the ridge tips in Lott

27 ver, excessive recoil pressure can produce a keyhole inside the melt pool, which is associated with g

28 g a transverse magnetic field suppresses the keyhole instability by driving a secondary thermoelectri

29 Keyhole instability during laser welding and laser powde

30 The critical keyhole instability generates acoustic waves in the melt

31 e rear keyhole wall is crucial in initiating keyhole instability.

32 ctylus punctatus), trematode parasites for a keyhole limpet (Fissurella latimarginata), and pinnother

33 Here, the unmineralized teeth of the giant keyhole limpet (Megathura crenulata) are shown to attain

34 for 19 species of the genus Haliotis plus a keyhole limpet and a more distantly related gastropod, t

35 xed with 150 mug GM-CSF) or control (100 mug keyhole limpet haemocyanin) via monthly intradermal inje

36 f an EGFRvIII-specific peptide conjugated to keyhole limpet haemocyanin.

37 -dependent antigen, 2,4-dinitrophenyl hapten-keyhole limpet hemocyanin (DNP(23)-KLH).

38 then conjugated to immunocyanin monomers of keyhole limpet hemocyanin (IC(KLH)) to create the MCV IC

39 ing of Id to the immunogenic carrier protein keyhole limpet hemocyanin (Id-KLH).

40 TCR Id protein conjugated to keyhole limpet hemocyanin (KLH) (TCR Id:KLH) and injecte

41 8) - when conjugated to the carrier protein, keyhole limpet hemocyanin (KLH) - to be capable of induc

42 B7RP-1-Fc stimulated the production of anti-keyhole limpet hemocyanin (KLH) Ab, increasing anti-KLH

43 ) followed by five subcutaneous boosts of Id/keyhole limpet hemocyanin (KLH) administered with adjuva

44 unoglobulin (Ig) idiotype (Id) conjugated to keyhole limpet hemocyanin (KLH) and administered with gr

45 This GM2 derivative was covalently linked to keyhole limpet hemocyanin (KLH) and monophosphoryl lipid

46 The DCs were pulsed with 2 foreign proteins, keyhole limpet hemocyanin (KLH) and tetanus toxoid (TT),

47 e to immunization with two conjugates, Tn(c)-keyhole limpet hemocyanin (KLH) and Tn(c)-palmitic acid

48 al, anti-idiotypic mAb MK2-23, conjugated to keyhole limpet hemocyanin (KLH) as a carrier and given w

49 ell as influenza matrix peptide (Flu-MP) and keyhole limpet hemocyanin (KLH) as control antigens.

50 Subjects were fed keyhole limpet hemocyanin (KLH) before subcutaneous immu

51 ts immunogenicity, we bound thiolated MEP to keyhole limpet hemocyanin (KLH) by using succinimidyl-4-

52 hat antibodies generated to the glycoprotein keyhole limpet hemocyanin (KLH) can cross-link with reac

53 ssful conjugation of the glycopeptide to the keyhole limpet hemocyanin (KLH) carrier protein complete

54 nthesis and conjugated to maleimide-modified keyhole limpet hemocyanin (KLH) carrier protein through

55 constant regions plus GM-CSF, or linkage to keyhole limpet hemocyanin (KLH) carrier protein were inc

56 To solve this problem, the keyhole limpet hemocyanin (KLH) conjugates of a series o

57 soluble Delta71-82 alphaS, human betaS, and keyhole limpet hemocyanin (KLH) control proteins induced

58 Volunteers were immunized with keyhole limpet hemocyanin (KLH) first orally and then pa

59 mor cell lysates and the immunogenic protein keyhole limpet hemocyanin (KLH) for 24 h and then combin

60 d, chemically synthesized, and conjugated to keyhole limpet hemocyanin (KLH) for examining its immuno

61 e C6 position (6OXY(Gly)(4)OH) conjugated to keyhole limpet hemocyanin (KLH) has shown early proof-of

62 ective antitumor immunity induced by s.c. Id-keyhole limpet hemocyanin (KLH) immunization.

63 n with 2,4,6-trinitrophenol (TNP)-conjugated keyhole limpet hemocyanin (KLH) in a specific pathogen-f

64 immunization with the cocaine immunogen GNC-keyhole limpet hemocyanin (KLH) in preventing cocaine se

65 ulsed with influenza matrix peptide (MP) and keyhole limpet hemocyanin (KLH) in two healthy subjects.

66 Mice immunized with the Ag keyhole limpet hemocyanin (KLH) mixed with HKL generated

67 econd-generation cocaine immunoconjugate GND-keyhole limpet hemocyanin (KLH) or with the anti-cocaine

68 (MyVax), comprising Id chemically coupled to keyhole limpet hemocyanin (KLH) plus granulocyte macroph

69 rotein conjugated to the immunogenic protein keyhole limpet hemocyanin (KLH) protects mice from tumor

70 on of the PI3P hapten to maleimide-activated keyhole limpet hemocyanin (KLH) provided a PI3P immunoge

71 igenic challenge of the transgenic mice with keyhole limpet hemocyanin (KLH) resulted in a decrease i

72 in animal models of inflammation including a keyhole limpet hemocyanin (KLH) study and a collagen-ind

73 re, the compounds demonstrated efficacy in a Keyhole Limpet Hemocyanin (KLH) study in rats, where the

74 was further conjugated to ovalbumin (OVA) or keyhole limpet hemocyanin (KLH) to enhance immunogenicit

75 was manufactured and covalently linked with keyhole limpet hemocyanin (KLH) to generate Id/KLH.

76 d to the immunogenic foreign carrier protein keyhole limpet hemocyanin (KLH) using glutaraldehyde has

77 efficacy by adding antimyeloma idiotype (Id)-keyhole limpet hemocyanin (KLH) vaccine to vaccine-speci

78 Keyhole limpet hemocyanin (KLH) was beneficial in earlie

79 o the peptides and to peptides conjugated to keyhole limpet hemocyanin (KLH) were characterized by th

80 different linker methods, to protein carrier keyhole limpet hemocyanin (KLH) were studied in mice.

81 d with peptide mimetics of GXM conjugated to keyhole limpet hemocyanin (KLH) with glutaraldehyde deve

82 T-independent (TNP-LPS) or T-dependent (TNP-keyhole limpet hemocyanin (KLH)) Ag.

83 Following challenge with TNP-keyhole limpet hemocyanin (KLH), Ab production in these

84 u-His-Gly) is conjugated to ovalbumin (OVA), keyhole limpet hemocyanin (KLH), and a bis-maleimide; KL

85 Rats were immunized with keyhole limpet hemocyanin (KLH), and blood samples were

86 ponse against an exogenous, nonself antigen, keyhole limpet hemocyanin (KLH), by releasing IL-4 in th

87 er the addition of a foreign helper protein, keyhole limpet hemocyanin (KLH), can augment the efficac

88 were gavaged with a single dose of 20 mg of keyhole limpet hemocyanin (KLH), followed by s.c. immuni

89 he globo H antigen conjugated to the protein keyhole limpet hemocyanin (KLH), has been in clinical ev

90 followed 4-6 weeks later by DCs pulsed with keyhole limpet hemocyanin (KLH), HLA-A*0201-positive res

91 in the primary response to PC conjugated to keyhole limpet hemocyanin (KLH), T15 Id(+) Abs constitut

92 nti-idiotypic mAb immunization protocol (mAb-keyhole limpet hemocyanin (KLH)-Calmette-Guerin bacillus

93 However, keyhole limpet hemocyanin (KLH)-priming of IFN-gko mice

94 c mice were cocultured with HDK-1 T cells (a keyhole limpet hemocyanin (KLH)-specific CD4+ Th1 clone)

95 MoPn), a nonprotective clone (N-MoPn), and a keyhole limpet hemocyanin (KLH)-specific cell line (KLH-

96 ere immunized with ovalbumin peptide or with keyhole limpet hemocyanin (KLH).

97 rotein conjugate, 2,4,6-trinitrophenyl (TNP)-keyhole limpet hemocyanin (KLH).

98 in mice 24 to 48 h before immunization with keyhole limpet hemocyanin (KLH).

99 usly with ovalbumin and a secondary antigen, keyhole limpet hemocyanin (KLH).

100 c IgY production following immunization with keyhole limpet hemocyanin (KLH).

101 b, 2C10, or vehicle before immunization with keyhole limpet hemocyanin (KLH).

102 ed with recombinant HPV16/18 E7 antigens and keyhole limpet hemocyanin (KLH; an immunological tracer

103 ith 4-hydroxy-3-nitrophenyl(5) conjugated to keyhole limpet hemocyanin (NP(5)- KLH) or infected with

104 e response to 4-hydroxy-3-nitrophenyl acetyl-keyhole limpet hemocyanin (NP-KLH) and NP-OVA develops w

105 hydroxy-3-nitrophenyl acetyl (NP)-conjugated keyhole limpet hemocyanin (NP-KLH) or ovalbumin(323-337)

106 se in mice primed with 2,4, 6-trinitrophenyl-keyhole limpet hemocyanin (TNP-KLH).

107 Intratumoral VVHY, VVGMCSF, and keyhole limpet hemocyanin (to produce CD4 help) generate

108 ubjected to disease-inducing (TNP-conjugated keyhole limpet hemocyanin [TNP-KLH]) and disease-inhibit

109 Inhibition of anti-keyhole limpet hemocyanin Ab response was dose-dependent

110 immunized with nitrophenol hapten-conjugated keyhole limpet hemocyanin adsorbed to Imject aluminum hy

111 rvivors mounted a substantial Ab response to keyhole limpet hemocyanin after completion of anti-CD40L

112 Moreover, mDCs(ICOS) pulsed with the keyhole limpet hemocyanin Ag during the maturation phase

113 es to alloantigen and secondary responses to keyhole limpet hemocyanin Ag.

114 ar versus vaccination with GM2 conjugated to keyhole limpet hemocyanin and administered with QS-21 (G

115 latimarginata hemocyanin in comparison with keyhole limpet hemocyanin and C. concholepas hemocyanin,

116 G antibody responses against protein antigen keyhole limpet hemocyanin and carbohydrate antigen sTn,

117 CD4+ T cell sensitization to keyhole limpet hemocyanin and CD8+ T cell sensitization

118 gainst 3-hydroxykynurenine (3OHKYN)-modified keyhole limpet hemocyanin and characterized it using 3OH

119 he immune responses to two soluble proteins, keyhole limpet hemocyanin and chicken egg albumin.

120 ne consisting of tumor Ig protein coupled to keyhole limpet hemocyanin and emulsified in an immunolog

121 Th2 immune deviation induced with keyhole limpet hemocyanin and IFA did not affect corneal

122 ations with cytokine-matured DCs loaded with keyhole limpet hemocyanin and MHC-I alone or MHC-I/II-re

123 ation to two different immunogenic carriers, keyhole limpet hemocyanin and N-alpha-palmitoyl-S-[2,3-b

124 sed humoral responses to the T-dependent Ags keyhole limpet hemocyanin and OVA, as well as reduced Ag

125 so inhibits production of antibodies against keyhole limpet hemocyanin and Pneumovax in mice, indicat

126 In response to trinitrophenol (TNP)-keyhole limpet hemocyanin and tetanus/diphtheria vaccine

127 impet hemocyanin or trinitrophenylated (TNP) keyhole limpet hemocyanin and the type 2 T-independent A

128 ne, or from the hybridoma, was conjugated to keyhole limpet hemocyanin and used to immunize Balb/c mi

129 domain of VlsE was conjugated to the carrier keyhole limpet hemocyanin and used to immunize mice.

130 sorbent assay and immunoblots using anti-AGE-keyhole limpet hemocyanin antibody, aminoguanidine inhib

131 al responses of L-selectin-deficient mice to keyhole limpet hemocyanin are indistinguishable from wil

132 Abs were induced after immunization with PC-keyhole limpet hemocyanin but at significantly lower lev

133 8+ alloreactive CTL, and development of anti-keyhole limpet hemocyanin CD4+ T cells, rejection of all

134 cious vaccine, MH6, was then contrasted with keyhole limpet hemocyanin conjugate vaccine in a subsequ

135 to mice immunized with the native 38C13 IgM-keyhole limpet hemocyanin conjugate vaccine.

136 vaccines (MH2[R], MH6, and MH7) or a control keyhole limpet hemocyanin conjugate vaccine.

137 Mice vaccinated with the CD20 peptide keyhole limpet hemocyanin conjugates had a 25% decrease

138 nd immunogenicity of three synthetic globo H-keyhole limpet hemocyanin conjugates plus the immunologi

139 Mice immunized with PA1 conjugated to keyhole limpet hemocyanin developed high anti-peptide (1

140 LS (SagA) propeptide [SLS(10-30)] coupled to keyhole limpet hemocyanin evoked antibodies in rabbits t

141 ation of naive mice with 3H1 conjugated with keyhole limpet hemocyanin Freund's adjuvant induced humo

142 h 8 injections using the standard therapy of keyhole limpet hemocyanin Id + GM-CSF.

143 ng 2,4,6-trinitrophenyl hapten conjugated to keyhole limpet hemocyanin immunization and nephritis ind

144 2,4,6-Trinitrophenyl hapten conjugated to keyhole limpet hemocyanin immunization resulted in highe

145 40L mRNA, antigen-specific IgG1 responses to keyhole limpet hemocyanin immunization, regulated CD4(+)

146 ncreased numbers of Th1 cells in response to keyhole limpet hemocyanin immunization.

147 Ficoll and in 4-hydroxy-3-nitrophenyl acetyl-keyhole limpet hemocyanin immunized animals; recall resp

148 timulate a T helper 2 response (ovalbumin or keyhole limpet hemocyanin in alum) and is only seen with

149 After immunization with OVA or keyhole limpet hemocyanin in CFA, NK cell-deficient (NK-

150 , 1,000-, or 100,000-mug doses of intranasal keyhole limpet hemocyanin in conjunction with adjuvant i

151 Efficacy experiments in a keyhole limpet hemocyanin model in rats demonstrated tha

152 Antibodies were raised by using keyhole limpet hemocyanin modified in vitro by 4-hydroxy

153 concurrent with a secondary Th2 response to keyhole limpet hemocyanin or A. fumagatus extract, or by

154 nd that loading immature DCs with the neoAgs keyhole limpet hemocyanin or human immunodeficiency viru

155 concurrent, secondary Th2 lung responses to keyhole limpet hemocyanin or primary responses to Nippos

156 -dependent (TD) Ags fluorescein-labeled (FL) keyhole limpet hemocyanin or trinitrophenylated (TNP) ke

157 lls from normal and B cell-deficient mice to keyhole limpet hemocyanin over 6 mo and observed diminis

158 ed toward Th2 responses by immunization with keyhole limpet hemocyanin plus IFA.

159 nd we have prepared a conjugate vaccine (GD2-keyhole limpet hemocyanin plus immunological adjuvant QS

160 ed from the original tumor, including (1) Id-keyhole limpet hemocyanin protein, (2) Id single-chain v

161 g rabbits with an F(2)Pab peptide coupled to keyhole limpet hemocyanin recognized a p53(1-39) peptide

162 Furthermore, CLEC12A-mediated delivery of keyhole limpet hemocyanin resulted in enhanced prolifera

163 ccinated with peptide 184- 198 conjugated to keyhole limpet hemocyanin showed significant pulmonary e

164 yl) form of ghrelin as compared with Ghr2 or keyhole limpet hemocyanin vaccinated controls.

165 y, delayed-type hypersensitivity response to keyhole limpet hemocyanin was diminished.

166 munogenicity of coupling the glycopeptide to keyhole limpet hemocyanin was examined; although both Ig

167 specific Abs following immunization with DNP-keyhole limpet hemocyanin was significantly decreased fo

168 of FDC networks, the primary Ab response to keyhole limpet hemocyanin was unaltered over a 20-day pe

169 responses to 2,4,6-trinitrophenyl-conjugated keyhole limpet hemocyanin were measured by ELISA, and pr

170 roduction of high-affinity antibodies to TNP-keyhole limpet hemocyanin were severely impaired, even a

171 ing 3 mg/kg iscalimab, antibody responses to keyhole limpet hemocyanin were transiently suppressed.

172 hesion to CR3 counterligands (fibrinogen and keyhole limpet hemocyanin) by 50%, but did not affect ad

173 (bacteriophage phiX 174 and nuclear protein-keyhole limpet hemocyanin) characterized by a reduction

174 nd proliferative response to recall antigen (keyhole limpet hemocyanin) were normal.

175 on of humoral immunity to model Ags (OVA and keyhole limpet hemocyanin), affecting all major T-depend

176 ella latimarginata, and Megathura crenulata (keyhole limpet hemocyanin), on cultures of peritoneal ma

177 Ag (keyhole limpet hemocyanin)-specific Th1/Th2 responses of

178 ed pulp by day 3 after immunization with Ars-keyhole limpet hemocyanin, (KLH) and at day 6, large clu

179 ccharide has been synthesized, conjugated to keyhole limpet hemocyanin, and administered with the imm

180 immunized with caffeine covalently linked to keyhole limpet hemocyanin, and recombinant antibody tech

181 These peptides were synthesized, coupled to keyhole limpet hemocyanin, and used to produce rabbit an

182 o the model Ag 4-hydroxy-3-nitrophenylacetyl-keyhole limpet hemocyanin, but GrB-deficient mice produc

183 es isolated from plasma of mice immunized to keyhole limpet hemocyanin, but not from naive or OVA-imm

184 result, when immunized with nitrophenylated-keyhole limpet hemocyanin, Dbc1(-/-) mice produce signif

185 When immunized with trinitrophenyl-keyhole limpet hemocyanin, dbh-/- mice produced less Th1

186 Immunization with DNP-keyhole limpet hemocyanin, heat-killed Brucella abortus,

187 the Ab response to the T cell-dependent Ag, keyhole limpet hemocyanin, in the PDE7A(-/-) mice was fo

188 Imaging of DNA, keyhole limpet hemocyanin, mouse monoclonal IgG, and glu

189 , IgM response to Pneumovax, IgG response to keyhole limpet hemocyanin, or cytokine response to LPS).

190 T-dependent Ag, phosphocholine conjugated to keyhole limpet hemocyanin, ppc1-5 NAA B cells mounted a

191 pulsing DCs with the foreign helper protein, keyhole limpet hemocyanin, prior to intratumoral deliver

192 Following vaccination with the TCR linked to keyhole limpet hemocyanin, specific anti-TCR humoral res

193 After immunization with trinitrophenyl-keyhole limpet hemocyanin, specific ASC could be isolate

194 d primary response to the T-dependent Ag DNP-keyhole limpet hemocyanin, the Tg mice exhibited severel

195 mary allergic sensitization to a neoantigen, keyhole limpet hemocyanin, using a unique model of human

196 ndent neoantigens, bacteriophage phiX174 and keyhole limpet hemocyanin, was also evaluated.

197 ing two recombinant filarial protein Ags and keyhole limpet hemocyanin, we sensitized T cells from un

198 decarboxylase (GAD), but not the control Ag keyhole limpet hemocyanin, were eliminated in NODJg mu(n

199 ystemically administered soluble protein Ag, keyhole limpet hemocyanin, were enhanced when mice were

200 man apoA-I, with or without conjugation with keyhole limpet hemocyanin, were fused with P3/NS1/1-Ag4-

201 of B7-H1Ig fusion protein, however, enhances keyhole limpet hemocyanin- specific T-cell proliferation

202 ient in Mac-1 were defective in adherence to keyhole limpet hemocyanin-coated glass, iC3b-mediated ph

203 7BL/6 mice were immunized with a cocktail of keyhole limpet hemocyanin-conjugated peptides correspond

204 sotypes distinct from those generated by the keyhole limpet hemocyanin-epitope conjugates.

205 nced proliferation and cytokine secretion by keyhole limpet hemocyanin-experienced CD4(+) T cells.

206 onor-specific Th2 cells, lymphoid cells from keyhole limpet hemocyanin-immune mice bearing healthy co

207 MR-1 in various preclinical models, such as keyhole limpet hemocyanin-induced Ab responses, alloanti

208 Guinea pigs immunized intranasally with a keyhole limpet hemocyanin-linked peptide, corresponding

209 VA-immunized mice, were able to suppress the keyhole limpet hemocyanin-specific delayed-type hypersen

210 f concanavalin A-stimulated spleen cells nor keyhole limpet hemocyanin-specific proliferation of sple

211 tion with LPS or upon 6-h coculture with the keyhole limpet hemocyanin-specific Th1 clone HDK-1 in th

212 3 to 24 h of incubation with HDK-1 T cells (keyhole limpet hemocyanin-specific TH1 clone) or with 5S

213 mice that were reconstituted with a clone of keyhole limpet hemocyanin-specific Th2 cells and trinitr

214 The sera raised against keyhole limpet hemocyanin-SV1 hapten, showed binding val

215 accharides were coupled with carrier protein keyhole limpet hemocyanin.

216 that had been immunized with trinitrophenyl-keyhole limpet hemocyanin.

217 bits (27- to 81-fold) after conjugation with keyhole limpet hemocyanin.

218 n with a thymus-dependent Ag, phosphocholine-keyhole limpet hemocyanin.

219 following immunization of male SJL mice with keyhole limpet hemocyanin.

220 eptides was increased by conjugating them to keyhole limpet hemocyanin.

221 uptake using FITC-labeled tetanus, OVA, and keyhole limpet hemocyanin.

222 tion, including host-restricted responses to keyhole limpet hemocyanin.

223 cell response against 2,4,6 trinitro-phenyl-keyhole limpet hemocyanin.

224 an isotype-matched control Ig, conjugated to keyhole limpet hemocyanin.

225 otetraose, or to oligosaccharides present on keyhole limpet hemocyanin.

226 njugate of sLe(a) with the benchmark carrier keyhole limpet hemocyanin.

227 single ascending dose groups challenged with keyhole limpet hemocyanin.

228 monas exotoxin A, as well as to the model Ag keyhole limpet hemocyanin.

229 zation with the T cell-dependent (TD) Ag DNP-keyhole limpet hemocyanin.

230 ice were similar after immunization with DNP-keyhole limpet hemocyanin.

231 coll and to the T cell-dependent antigen TNP-keyhole limpet hemocyanin.

232 s immunized with UO(2)(2+)-DCP conjugated to keyhole limpet hemocyanin.

233 ing of lymphoma immunoglobulin conjugated to keyhole limpet hemocyanin.

234 n a mammalian cell and chemically coupled to keyhole limpet hemocyanin.

235 Cys-27-NH2 as a hapten, conjugated to BSA or keyhole limpet hemocyanin.

236 strong suppression of IgE in response to DNP-keyhole limpet hemocyanin/alum and Nippostrongylus brasi

237 er, pulsing MoDC with conjugates of primary (keyhole limpet hemocyanin; KLH) and recall (Bet v 1) Ags

238 nd linked GH to a carrier protein, including keyhole limpet hemocyanion, diphtheria toxoid cross-reac

239 ith the phase III clinical trial vaccine, GH-keyhole limpet hemocyanion/QS21, the GH-DT/C34 vaccine e

240 GNE-KLH (keyhole limpet hemocyannin) was found to elicit persiste

241 st as much as the more obvious outgroup, the keyhole limpet, an observation common to other DNA seque

242 Focusing on keyhole limpets, genera Fissurella and Diodora from Cape

243 Within the three cell type cluster complex, keyhole limpit hemocyanin or tetanus toxoid-reactive Th

244 Both keyhole lymphet hemocyanin conjugates induced IgM and Ig

245 these constructs as free glycopeptides or as keyhole lymphet hemocyanin conjugates.

246 ses to NP-KLH (4-hydroxy-3-nitrophenylacetyl/keyhole lymphocyte hemocyanin) immunization.

247 y of the full-Fourier image, whereas the 50% keyhole method degraded the spatial resolution by a fact

248 usion zones, the direct visualization of the keyhole morphology and dynamics with high-energy x-rays

249 morphological transition from stable at low Keyhole number to chaotic at high Keyhole number.

250 We define a dimensionless number, the Keyhole number, to predict aspect ratio of a keyhole and

251 ble at low Keyhole number to chaotic at high Keyhole number.

252 sics simulations, we discovered two types of keyhole oscillation in laser powder bed fusion of Ti-6Al

253 is minimizes protrusions and large-amplitude keyhole oscillations.

254 mong clamp proteins and exhibits a "key in a keyhole" pattern where a bulky aromatic residue from one

255 In particular, the keyhole pore formation is experimentally revealed with h

256 manufacturing (AM), process defects such as keyhole pores are difficult to anticipate, affecting the

257 he findings support the hypotheses that: (i) keyhole porosity can initiate not only in unstable, but

258 However, some keyhole porosity formation mechanisms, e.g., keyhole flu

259 ped an approach for detecting the stochastic keyhole porosity generation events with submillisecond t

260 Keyhole porosity is a key concern in laser powder-bed fu

261 We found that the boundary of the keyhole porosity regime in power-velocity space is sharp

262 pattern was used to reduce the formation of keyhole porosity, which was caused by excessive vaporiza

263 , spatter generation, and crack formation at keyhole porosity.

264 Our findings indicate that the short keyhole rear wall, the high backward melt velocity, and

265 only in unstable, but also in the transition keyhole regimes created by high laser power-velocity con

266 s the symmetry-breaking into this triangular keyhole shape.

267 d an intermediate characteristic "triangular keyhole" shape in the 3D deformations of the hindgut.

268 Catheter placement via the supraorbital keyhole (SOK) for removing spontaneous intracerebral hem

269 Radiography showed extensive keyholing, spatter generation, and crack formation at ke

270 re, we discover inherent correlation between keyhole stability and porosity formation in metal 3D pri

271 entify simple yet universal scaling laws for keyhole stability and porosity in metal 3D printing.

272 cervical hysterectomy involves laparoscopic (keyhole) surgery to remove the upper part of the uterus

273 aker technique had less recurrences than the keyhole technique (OR 2.3, 95% CI 1.2-4.6; P = 0.016).

274 iled gradient-recalled-echo imaging with the keyhole technique during the administration of 0.1 mmol/

275 he Sugarbaker technique is superior over the keyhole technique showing fewer recurrences.

276 t vital driving force for the pores near the keyhole tip to move away from the keyhole and become tra

277 l-4V caused by a critical instability at the keyhole tip.

278 terize the evolution of the melt pool shape, keyhole, vapor plume, and thermal evolution in Ti-6Al-4V

279 e flow vortex-induced protrusion on the rear keyhole wall is crucial in initiating keyhole instabilit

280 ith deep and narrow vapor depressions called keyholes, which occur under high-power, low-scan speed l

281 leoside is located in the narrow part of the keyhole, while the sugar occupies the wider opening.